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Does prior traumatization affect the treatment outcome of CBT for panic disorder? The potential role of the MAOA gene and depression symptoms.

Does prior traumatization affect the treatment outcome of CBT for panic disorder? The potential role of the MAOA gene and depression symptoms.
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Trautmann S, Richter J, Muehlhan M, Höfler M, Wittchen HU, Domschke K, Ströhle A, Hamm AO, Weber H, Kircher T, Arolt V, Gerlach AL, Alpers GW, Fydrich T, Lang T, Reif A,


Trautmann S, Richter J, Muehlhan M, Höfler M, Wittchen HU, Domschke K, Ströhle A, Hamm AO, Weber H, Kircher T, Arolt V, Gerlach AL, Alpers GW, Fydrich T, Lang T, Reif A, (click to view)

Trautmann S, Richter J, Muehlhan M, Höfler M, Wittchen HU, Domschke K, Ströhle A, Hamm AO, Weber H, Kircher T, Arolt V, Gerlach AL, Alpers GW, Fydrich T, Lang T, Reif A,

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European archives of psychiatry and clinical neuroscience 2017 07 15() doi 10.1007/s00406-017-0823-9
Abstract

Although cognitive behavioral therapy (CBT) is highly effective in the treatment of anxiety disorders, many patients still do not benefit. This study investigates whether a history of traumatic event experience is negatively associated with outcomes of CBT for panic disorder. The moderating role of the monoamine oxidase A (MAOA) gene and depression symptoms as well as the association between trauma history and fear reactivity as a potential mechanism are further analyzed. We conducted a post-hoc analysis of 172 male and 60 female patients with panic disorder treated with CBT in a multi-center study. Treatment outcome was assessed at post-treatment using self-report and clinician rating scales. Fear reactivity before treatment was assessed via heart rate and self-reported anxiety during a behavioral avoidance test. Among females, we did not find any differences in treatment response between traumatized and non-traumatized individuals or any two-way interaction trauma history × MAOA genotype. There was a significant three-way interaction trauma history × MAOA genotype × depression symptoms on all treatment outcomes indicating that in traumatized female patients carrying the low-activity allele, treatment effect sizes decreased with increasing depression symptoms at baseline. No such effects were observed for males. In conclusion, we found no evidence for a differential treatment response in traumatized and non-traumatized individuals. There is preliminary evidence for poorer treatment outcomes in a subgroup of female traumatized individuals carrying the low-active variant of the MAOA gene. These patients also report more symptoms of depression symptomatology and exhibit a dampened fear response before treatment which warrants further investigation.

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